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AbbVie ENFit NJ

EUDAMED

Class IIa (EU MDR)

Ref 0AV094-003Model 0AV094

by AbbVie Inc.

Identity

Trade Name
AbbVie ENFit NJ EUDAMED
Device Name
AbbVie ENFit NJ EUDAMED
Model / Reference
0AV094 EUDAMED
0AV094-003 EUDAMED

Identifiers

Primary DI / UDI-DI
08054083029511 EUDAMED
Basic UDI-DI
8054083000V0AV094XE EUDAMED
EMDN Code
G02020102 NASOJEJUNAL/NASODUODENAL TUBES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Estonia EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

AbbVie ENFit NJ by Abbvie Inc. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
AbbVie Inc.
EUDAMED SRN
US-MF-000014055
Authorised Representative
Allergan Pharmaceuticals International Limited IE-AR-000000650

Sources (1)

  • EUDAMED 8cee5321-4aa3-49db-bb01-ba8ddfbd4a17 61 fields · synced Jul 24, 2026